These findings represent an important step towards a better understanding of human Leishmania infection, with relevance to
parasite drug resistance, pathogenicity, and tissue tropism.
Scientists have uncovered a potential mode of
parasite drug resistance in malaria infection, according to a report published in The Journal of Experimental Medicine.
Not exact matches
And the
parasite that causes malaria is gaining
resistance to some of the best
drugs used to treat the disease, including artemisinin.
Treating malaria with chloroquine is no longer a viable option for most people as the
parasite has developed
resistance to the
drug.
H. contortus has become resistant to all major treatments against parasitic worms, so its genome is a good model to understand how
drug resistance develops in this complex group of closely related
parasites and will also reveal further potential
drug and vaccine targets.
Scientists have made a major breakthrough in the global search for a new
drug to beat the malaria
parasite's growing
resistance to first - defence treatments.
Using the latest molecular biology techniques, Myrick hopes to understand
drug resistance in the
parasite that causes the disease.
Former mainstay
drugs (chloroquine and sulfadoxine — pyrimethamine) also experienced their first
resistance challenges in western Cambodia before spreading to other parts of Asia and on to Africa, where the
parasites killed millions.
From the outset, a few scientists questioned whether what the group described was really
drug resistance or should instead be called «slow clearance» of the
parasite — and some even accused the Mahidol group of crying wolf.
Both groups confirmed in genetic, cell, and clinical studies that, for the first time, the
parasite had developed
resistance to both
drugs used in an ACT.
Another team from the University of Washington discovered that the malaria
parasite in Asia outsmarts
drugs and develops
resistance much more quickly than in other parts of the world.
The finding that hemozoin formation is not essential for
parasite survival in reticulocytes suggests that the
parasites can develop different means of survival in the blood affording them certain
drug resistance.
Given the emergence of artemisinin
resistance, these findings could potentially lead to the design of new treatments against
drug - resistant
parasites.
At AAAS, a researcher describes how treating more people for the mosquito - borne
parasite could lead to more
resistance to
drugs
Biologists in Britain say that they have evidence that the
parasite Schistosoma mansoni, which causes schistosomiasis, can develop
resistance to the
drug praziquantel.
We've already moved away from using quinine to treat cases as the malaria
parasite has become more resistant to it, but if further
drug resistance were to develop against our most valuable malaria
drug, artemisinin, we would be facing a grave situation.
The current results, however, may not hold true in all areas because risk of malaria transmission varies according to location, as does
parasite resistance to
drugs.
By now, some
parasites have evolved
resistance to the
drug: genetic adaptations that allow them to expel chloroquine from their food vacuoles 40 to 50 times faster than their
drug - sensitive kin.
«The over-prescribing of anti-malarials puts evolutionary pressure on the malaria
parasite that risks hastening its
resistance to artemisinin - based combination therapy — the frontline
drugs used to treat malaria in Africa,» Stoler said.
Resistance to antibiotics to tackle bacterial infections and antimicrobial
drugs used to treat
parasites, viruses and fungi is spreading at an alarming rate.
«Researchers assess use of
drug - susceptible
parasites to fight
drug resistance.»
The strategy would take advantage of
parasite refugia — host populations that have not been treated with
drugs, thereby serving as «safe zones» where
parasites don't develop
drug resistance.
Growing
resistance to malaria
drugs in Southeast Asia is caused by a single mutated gene inside the disease - causing Plasmodium falciparum
parasite, according to a study led by David Fidock, PhD, professor of microbiology & immunology and of medical sciences (in medicine) at Columbia University Medical Center.
A study published on June 25th in PLOS Pathogens reports a new way to circumvent
drug resistance and lower the curative dose by delivering existing
drugs directly into the
parasite, a high - tech approach with potential applications to other infectious diseases.
Like for many neglected tropical diseases that disproportionately affect poor populations, existing
drugs have serious side - effects and face increasing
parasite resistance.
The existing
drugs have serious side effects, and the
parasites are developing
resistance.
The findings suggest that other antimalarial medications that target maternally inherited organelles in the
parasite may also have limited
drug resistance.
Over the decades, malaria
parasites have developed
resistance to almost every
drug humans have thrown at them.
This is possible because quinolines are active inside a cell organelle called the digestive vacuole;
resistance occurs when the
parasite finds ways of keeping the
drug out of the vacuole.
Letting
parasites fight could help battle
drug resistance, too.
Current antimalarial
drugs are becoming less effective as the
parasite develops
resistance to the
drugs, making the search for new targets that can kill all species of malaria critical.
Genetic variation in antigenic,
drug resistance, and pathogenesis determinants is abundant, consistent with an ancient origin of P. falciparum, whereas DNA variation at silent (synonymous) sites in coding sequences appears virtually absent, consistent with a recent origin of the
parasite.
In the early 2000s, the malaria
parasite Plasmodium falciparum developed
resistance to the commonly used antimalarial
drug chloroquine.
«As
drug resistance is a major problem for malaria control and eradication, it is critical that that we continue to develop new antimalarials that act against previously unexploited targets in the
parasite to keep priming the
drug pipeline.»
Diversifying the antimalarial arsenal could also extend the lifespan of existing
drugs, since relying less heavily on our most commonly used weapons gives the
parasite fewer opportunities to develop
resistance, Derbyshire said.
Resistance to
drug treatments is spreading among the
parasite's many strains, and researchers are working hard to find new
drug targets.
The meeting explored the genomic epidemiology of the host, vector and
parasite, highlighting the practical relevance of this research to global health, including antimalarial
drug resistance, insecticide
resistance, vaccine design, and mechanisms of protective immunity.
The awards span the broad mission of the NIH and include groundbreaking research, such as engineering immune cells producing
drugs at the site of diseased tissue; developing a sensor to rapidly detect antibiotic
resistance of a bacterial infection; understanding how certain
parasites evade host detection by continually changing their surface proteins; and developing implants that run off the electricity generated from the motion of a beating the heart.
A team from the University of Melbourne has been honoured with an «Oscar of science» — the Australian Museum's annual science award, the Eureka Prize — for its work on
drug resistance in malaria
parasites.
A new technique has been developed to identify hotspots of malaria
parasite evolution and track the rise of malarial
drug resistance, faster and more efficiently than ever before.
In addition, they observed that
parasites with multiple copies of the multidrug
resistance gene pfmdr1 tended to be less susceptible to several
drugs, including DHA.
A team from the University of Melbourne has reached the finals of the «Oscars of science» — the Australian Museum's annual science award, the Eureka Prize — for its work on
drug resistance in malaria
parasites.
The most comprehensive genetic study of malaria
parasites in Southeast Asia has shown that
resistance to antimalarial
drugs was under - reported for years in Cambodia.
Topics this year include genomic epidemiology of the host, vector and
parasite, highlighting the practical relevance of this research to global health, including anti-malarial
drug resistance, insecticide
resistance, vaccine design, and mechanisms of protective immunity.
Researchers from 23 institutions spanning South East Asia, Africa, the USA and UK sequenced
parasite genomes from more than 800 malaria samples from Africa and from South East Asia, with the aim of investigating how genetic monitoring of malaria on a large scale could identify and track
drug -
resistance.
Using new genome sequencing technologies, the researchers discovered multiple strains of the malaria - causing
parasite Plasmodium falciparum that appear to be rapidly expanding throughout the local
parasite population in Western Cambodia, a known hotspot for
drug resistance.
A worldwide collaboration of researchers has shown that
resistance to the frontline antimalarial
drug — artemisinin — can be identified by surveying the genomes of
parasite populations.
Ultimately, the goals are to develop cost - effective genetic tools to determine whether a patient is carrying
parasites that are
drug resistant; to map the emergence of
resistance; to understand the mechanisms and routes of spread of
resistance; and to plan the most effective strategy to control and eliminate the problem.
«By understanding how the environment in which the
parasite lives influences its susceptibility to
drugs and the molecular mechanisms of
drug resistance, we hope to be able to develop new intervention strategies to combat visceral leishmaniasis in Brazil.»
Each time a new antimalarial
drug has been introduced, the
parasites have evolved
resistance to it.